STRYKER NAVIGATION SYSTEM - HIP MODULE
FDA 510(k) clearance K022365 · decided 2003-01-22
Clearance details
- K-number
- K022365
- Device name
- STRYKER NAVIGATION SYSTEM - HIP MODULE
- Applicant
- Stryker Instruments
- Decision
- Substantially Equivalent
- Date received
- 2002-07-22
- Decision date
- 2003-01-22
- Days to decision
- 184 days
- Clearance type
- Traditional
- Product code
- HAW
- Device class
- 2
- Regulation number
- 882.4560
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Kalamazoo, MI, US
- Third-party review
- No
- Expedited review
- No
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